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87,000+ live jobsPhysicochemical Quality Control Analyst
On-site in Azuqueca de Henares·Full-time·Added 20 days ago (last checked 2 Nov)
Insud Pharma
61 open roles
Our summary
- Hours
- Rotating shifts, including nights
- Work mode
- On-site, Azuqueca de Henares
- Contract
- Permanent, full-time hours
- Education
- Higher vocational training (FP Grado Superior)
- Benefits
- Life insurance
Visa options
The ad doesn’t mention sponsorship
Not a refusal, but not a yes. Worth asking in your first message.
Skills
Nice to have
This job advert was originally written in Spanish.
Requirements
What we're looking for
- Education: Higher Degree in Analysis and Quality Control or similar.
- Experience (years/area): +1 years of experience in a pharmaceutical laboratory in the Quality Control area, preferably in Injectables.
Nice to have
- Desirable: knowledge of Office Software at user level and basic English level. Experience in HPLC and GC using Empower software.
Pay & benefits
What you'll get
⏰Rotating schedule: mornings 06:00 to 14:00, afternoons 14:00 to 22:00, and nights 22:00 to 06:00
📜Permanent contract
💸Salary based on merit (fixed salary + rotation bonus + night shift bonus)
🥼 Life and accident insurance.
🥼 Co-payment for voluntary health insurance.
💸Benefits and Savings Club.
📈Development plans, internal mobility policy.
⭐And many more!
The role
Position: Physico-Chemical Quality Control Analyst
Location: Azuqueca de Henares
Experience: at least 2 years in similar roles
Follow us on social networks such as LinkedIn/Instagram and stay tuned to any offers we release; the opportunity to be a new Insuder is waiting!
#InsudPharma #Challenger #Insuder #InsudTalent
What you'll do
Take samples and analyze, using different analytical techniques (GC, HPLC, TLC, KF), APIs, intermediate samples, or final samples, completing the work sheets for each product and performing verifications of HPLC, GC, KF, and Analytical Balances; GMPs in accordance with the Standards, the guidelines of the Standard Operating Procedures (SOPs) regarding the weekly cleaning of the work area and the supervisor; in order to ensure the good quality (compliance with specifications) of the different products, ensure the proper functioning of the equipment, and facilitate decision-making for supervisors. All this while taking into account the safety rules indicated by the company and the use of the personal protective equipment provided based on the risks of each operation.
- Perform analyses of water, raw materials, intermediate products, finished products, and primary and secondary packaging material.
- Perform analyses related to analytical method transfers.
- Evaluation, reporting of data and results.
- Follow the established documentation for the execution of tasks in the Laboratory (standard operating procedures, supporting documentation, manuals, etc.) and GxP working systematics.
- Contribute to guaranteeing the state of training control required in their area of responsibility (specific technique, GxP, safety, etc.).
- Collaborate for the correct development of GMP regulatory inspections, customer audits, and the execution of the self-inspection program.
- Collaborate in maintaining the proper state of order and cleanliness of the Laboratory.
- Manage laboratory reagents, materials, and standards.
- Perform daily verifications of the required equipment.
- Follow work rules (including order and cleanliness) and established procedures.
- Participate in investigations, OOS, and OOT.
What are we looking for? 🔎
The challenge!
What do you need?
- Personal skills: good organizational and problem-solving capacity, teamwork, initiative, and decision-making.
- Technical skills: ability to work in a regulated environment.
Our benefits!
Hiring process
➡️Keep an eye on your phone and email! Most likely, the first thing we will do is contact you through one of these two channels.
➡️Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be between one and two interviews in the process and, depending on the type of process, there may also be some type of test.
➡️Wait for the result! We care about ensuring that you feel guided in every selection process and know what to expect from us, so we will endeavor to always indicate the status of the process to you.
About Insud Pharma
- Industry
- Pharmaceuticals
In their own words
About the company & team
INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and expertise in scientific research, development, manufacturing, sale, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health.
INSUD PHARMA's activity is organized into three synergistic business areas: Industrial, Branded, and Biotech, with more than 10,000 professionals in over 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development.
We are incorporating a new INSUDER as a Physico-Chemical Quality Control Analyst in our injectables plant located in Azuqueca de Henares.
Additional information
The InsudPharma group is aware that business management must be in line with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as set out in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.
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